PEX11β deficiency is lethal and impairs neuronal migration but does not abrogate peroxisome function

Molecular and Cellular Biology

Volumn 22, Issue 12, 2002, Pages 4358-4365

  Li, Xiaoling ^a   Baumgart, Eveline ^a   Morrell, James C ^a   Jimenez Sanchez, Gerardo ^a   Valle, David ^a   Gould, Stephen J ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; PROTEIN PEX11BETA; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CELL FUNCTION; CELL METABOLISM; CELL MIGRATION; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; EMBRYO; ENZYME DEFICIENCY; ENZYME LOCALIZATION; GENE DISRUPTION; KNOCKOUT MOUSE; LETHALITY; MOUSE; MUSCLE HYPOTONIA; NERVE CELL; NONHUMAN; PEROXISOME; PHENOTYPE; PRIORITY JOURNAL; PROTEIN TRANSPORT; ZELLWEGER SYNDROME;

ANIMALS; CELL MOVEMENT; FATTY ACIDS; FETAL GROWTH RETARDATION; HUMANS; MEMBRANE PROTEINS; MICE; MICE, INBRED C57BL; MICE, MUTANT STRAINS; MITOCHONDRIA; MUSCLE HYPOTONIA; NEURONS; PEROXISOMES; PROTEIN TRANSPORT; ZELLWEGER SYNDROME;

ANIMALIA;

EID: 0036261777     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.22.12.4358-4365.2002     Document Type: Article

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